Genomic variant #0000795422

Individual ID 00000003
Chromosome 21
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.14274076A>G
Reference dbSNP
DB-ID ABCC13_000002
Frequency 0.858
Allele Count 182
Allele Number 212
Depth 2905
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
ABCC13 NR_003087.1 ./.
ABCC13 NR_003088.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin